Verhagen J, Veldink G A, Egmond M R, Vliegenthart J F, Boldingh J, van der Star J
Biochim Biophys Acta. 1978 Jun 23;529(3):369-79. doi: 10.1016/0005-2760(78)90081-4.
The steady-state kinetics of the anaerobic reaction of soybean lipoxygenase-1 with linoleic acid and 13-L-hydroperoxylinoleic acid were studied. Initial rates of the formation of oxodienoic acids**, absorbing at 285 nm, were measured at pH 10. About 50% of the consumed 13-L-hydroperoxylinoleic acid was converted into oxodienoic acids regardless of the initial ratio of the two substrates. A linear inhibition by both linoleic acid and 13-L-hydroperoxylinoleic acid was observed in the concentration range studied, which is on the upper side limited by the concentrations at which micelle- or acid-soap formation starts. A kinetic scheme is proposed based on one active site in lipoxygenase-1 which alternately binds the two substrates. Values for the kinetic constants were calculated by fitting simultaneously the complete set of data to the appropriate rate equation.
研究了大豆脂氧合酶-1与亚油酸和13-L-氢过氧亚油酸厌氧反应的稳态动力学。在pH 10下测量了在285 nm处有吸收的氧代二烯酸**形成的初始速率。无论两种底物的初始比例如何,约50%消耗的13-L-氢过氧亚油酸转化为氧代二烯酸。在所研究的浓度范围内观察到亚油酸和13-L-氢过氧亚油酸均呈线性抑制,该浓度范围上限受胶束或酸皂形成起始浓度限制。基于脂氧合酶-1中一个交替结合两种底物的活性位点提出了一个动力学方案。通过将完整数据集同时拟合到适当的速率方程来计算动力学常数的值。